Hereditary angioedema: quality of life in Brazilian patients

Detalhes bibliográficos
Autor(a) principal: Gomide, Maria Abadia Consuelo M. S.
Data de Publicação: 2013
Outros Autores: Toledo, Eliana, Valle, Solange Oliveira Rodrigues, Campos, Regis A., França, Alfeu T., Gomez, Nieves Prior, Andrade Jr., Heitor Franco, Caballero, Teresa, Grumach, Anete S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/52321
Resumo: OBJECTIVE: Hereditary angioedema is a serious medical condition caused by a rare autosomal dominant genetic disorder and it is associated with deficient production or dysfunction of the C1 esterase inhibitor. In most cases, affected patients experience unexpected and recurrent crises of subcutaneous, gastrointestinal and laryngeal edema. The unpredictability, intensity and other factors associated with the disease impact the quality of life of hereditary angioedema patients. We evaluated the quality of life in Brazilian hereditary angioedema patients. METHODS: Patients older than 15 years with any severity of hereditary angioedema and laboratory confirmation of C1 inhibitor deficiency were included. Two questionnaires were used: a clinical questionnaire and the SF-36 (a generic questionnaire). This protocol was approved by the Ethics Committee of Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo. RESULTS: The SF-36 showed that 90.4% (mean) of all the patients had a score below 70 and 9.6% had scores equal to or higher than 70. The scores of the eight dimensions ranged from 51.03 to 75.95; vitality and social aspects were more affected than other arenas. The internal consistency of the evaluation was demonstrated by a Cronbach's alpha value above 0.7 in seven of the eight domains. CONCLUSIONS: In this study, Brazilian patients demonstrated an impaired quality of life, as measured by the SF-36. The most affected domains were those related to vitality and social characteristics. The generic SF-36 questionnaire was relevant to the evaluation of quality of life; however, there is a need for more specific instruments for better evaluation.
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spelling Hereditary angioedema: quality of life in Brazilian patients Hereditary AngioedemaQuality of LifeQuestionnairesSF-36Asphyxia OBJECTIVE: Hereditary angioedema is a serious medical condition caused by a rare autosomal dominant genetic disorder and it is associated with deficient production or dysfunction of the C1 esterase inhibitor. In most cases, affected patients experience unexpected and recurrent crises of subcutaneous, gastrointestinal and laryngeal edema. The unpredictability, intensity and other factors associated with the disease impact the quality of life of hereditary angioedema patients. We evaluated the quality of life in Brazilian hereditary angioedema patients. METHODS: Patients older than 15 years with any severity of hereditary angioedema and laboratory confirmation of C1 inhibitor deficiency were included. Two questionnaires were used: a clinical questionnaire and the SF-36 (a generic questionnaire). This protocol was approved by the Ethics Committee of Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo. RESULTS: The SF-36 showed that 90.4% (mean) of all the patients had a score below 70 and 9.6% had scores equal to or higher than 70. The scores of the eight dimensions ranged from 51.03 to 75.95; vitality and social aspects were more affected than other arenas. The internal consistency of the evaluation was demonstrated by a Cronbach's alpha value above 0.7 in seven of the eight domains. CONCLUSIONS: In this study, Brazilian patients demonstrated an impaired quality of life, as measured by the SF-36. The most affected domains were those related to vitality and social characteristics. The generic SF-36 questionnaire was relevant to the evaluation of quality of life; however, there is a need for more specific instruments for better evaluation. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2013-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/5232110.6061/clinics/2013(01)OA13Clinics; v. 68 n. 1 (2013); 81-83 Clinics; Vol. 68 Núm. 1 (2013); 81-83 Clinics; Vol. 68 No. 1 (2013); 81-83 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/52321/56348Gomide, Maria Abadia Consuelo M. S.Toledo, ElianaValle, Solange Oliveira RodriguesCampos, Regis A.França, Alfeu T.Gomez, Nieves PriorAndrade Jr., Heitor FrancoCaballero, TeresaGrumach, Anete S.info:eu-repo/semantics/openAccess2013-03-09T14:08:18Zoai:revistas.usp.br:article/52321Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2013-03-09T14:08:18Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Hereditary angioedema: quality of life in Brazilian patients
title Hereditary angioedema: quality of life in Brazilian patients
spellingShingle Hereditary angioedema: quality of life in Brazilian patients
Gomide, Maria Abadia Consuelo M. S.
Hereditary Angioedema
Quality of Life
Questionnaires
SF-36
Asphyxia
title_short Hereditary angioedema: quality of life in Brazilian patients
title_full Hereditary angioedema: quality of life in Brazilian patients
title_fullStr Hereditary angioedema: quality of life in Brazilian patients
title_full_unstemmed Hereditary angioedema: quality of life in Brazilian patients
title_sort Hereditary angioedema: quality of life in Brazilian patients
author Gomide, Maria Abadia Consuelo M. S.
author_facet Gomide, Maria Abadia Consuelo M. S.
Toledo, Eliana
Valle, Solange Oliveira Rodrigues
Campos, Regis A.
França, Alfeu T.
Gomez, Nieves Prior
Andrade Jr., Heitor Franco
Caballero, Teresa
Grumach, Anete S.
author_role author
author2 Toledo, Eliana
Valle, Solange Oliveira Rodrigues
Campos, Regis A.
França, Alfeu T.
Gomez, Nieves Prior
Andrade Jr., Heitor Franco
Caballero, Teresa
Grumach, Anete S.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Gomide, Maria Abadia Consuelo M. S.
Toledo, Eliana
Valle, Solange Oliveira Rodrigues
Campos, Regis A.
França, Alfeu T.
Gomez, Nieves Prior
Andrade Jr., Heitor Franco
Caballero, Teresa
Grumach, Anete S.
dc.subject.por.fl_str_mv Hereditary Angioedema
Quality of Life
Questionnaires
SF-36
Asphyxia
topic Hereditary Angioedema
Quality of Life
Questionnaires
SF-36
Asphyxia
description OBJECTIVE: Hereditary angioedema is a serious medical condition caused by a rare autosomal dominant genetic disorder and it is associated with deficient production or dysfunction of the C1 esterase inhibitor. In most cases, affected patients experience unexpected and recurrent crises of subcutaneous, gastrointestinal and laryngeal edema. The unpredictability, intensity and other factors associated with the disease impact the quality of life of hereditary angioedema patients. We evaluated the quality of life in Brazilian hereditary angioedema patients. METHODS: Patients older than 15 years with any severity of hereditary angioedema and laboratory confirmation of C1 inhibitor deficiency were included. Two questionnaires were used: a clinical questionnaire and the SF-36 (a generic questionnaire). This protocol was approved by the Ethics Committee of Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo. RESULTS: The SF-36 showed that 90.4% (mean) of all the patients had a score below 70 and 9.6% had scores equal to or higher than 70. The scores of the eight dimensions ranged from 51.03 to 75.95; vitality and social aspects were more affected than other arenas. The internal consistency of the evaluation was demonstrated by a Cronbach's alpha value above 0.7 in seven of the eight domains. CONCLUSIONS: In this study, Brazilian patients demonstrated an impaired quality of life, as measured by the SF-36. The most affected domains were those related to vitality and social characteristics. The generic SF-36 questionnaire was relevant to the evaluation of quality of life; however, there is a need for more specific instruments for better evaluation.
publishDate 2013
dc.date.none.fl_str_mv 2013-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/52321
10.6061/clinics/2013(01)OA13
url https://www.revistas.usp.br/clinics/article/view/52321
identifier_str_mv 10.6061/clinics/2013(01)OA13
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/52321/56348
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; v. 68 n. 1 (2013); 81-83
Clinics; Vol. 68 Núm. 1 (2013); 81-83
Clinics; Vol. 68 No. 1 (2013); 81-83
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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